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别名 AZ-82, AZ 82
AZ82 是一种具有选择性和高效性的驱动蛋白样蛋白 KIFC1 抑制剂,抑制 PCa 细胞胞质和细胞核中 KIFC1 的表达,诱导前列腺癌细胞多极有丝分裂和细胞凋亡。

AZ82 是一种具有选择性和高效性的驱动蛋白样蛋白 KIFC1 抑制剂,抑制 PCa 细胞胞质和细胞核中 KIFC1 的表达,诱导前列腺癌细胞多极有丝分裂和细胞凋亡。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 699 | In Stock |
AZ82 相关产品
| 产品描述 | AZ82 is a selective and potent inhibitor of the kinesin-like protein KIFC1, inhibits KIFC1 expression in the cytoplasm and nucleus of PCa cells, and induces multipolar mitosis and apoptosis in prostate cancer cells. |
| 靶点活性 | HSET/KIFC1:300 nM, HSET/KIFC1:43 nM (Ki), HSET/KIFC1:43 nM (ki) |
| 体外活性 | AZ82 specifically induce multipolar spindles in BT-549 cells, but not in cancer cells with normal centrosome numbers, such as HeLa [1]. AZ82 binds specifically to KIFC1/MT complex but not to KIFC1 or MT alone. Treatment with AZ82 caused centrosome declustering in BT-549 breast cancer cells with amplified centrosomes. AZ82 inhibits both processes for mant-ATP binding/releasing (IC50: 0.90 μM/1.26 μM) [2]. |
| 别名 | AZ-82, AZ 82 |
| 分子量 | 560.63 |
| 分子式 | C28H31F3N4O3S |
| CAS No. | 1449578-65-7 |
| Smiles | CCCc1cc(sc1C)C(=O)N[C@H](Cc1ccc(nc1)-c1cccc(OC(F)(F)F)c1)C(=O)N[C@@H]1CCNC1 |
| 密度 | 1.32 g/cm3 (Predicted) |
| 存储 | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 100 mg/mL (178.37 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
| 体内实验配方 | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (7.13 mM), Sonication is recommended. 请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。 | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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